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Impact of - IDL-BNC @ IDRC - International Development Research ...

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(Inauguration speeches, Agricultural University, Wageningen, 1976, unpublished)<br />

point out that selectivity can also be improved by choosing the optimum<br />

time, place, and method <strong>of</strong> application; by improving the formulation;<br />

and by mixing a pesticide with other chemicals.<br />

In certain cases, higher pesticidal activity can also be achieved by removing<br />

the less-active optical isomers (e.g., in pyrethroids) or less-active and nonactive<br />

components (e.g., removing 1,2-dichloropropane from a mixture <strong>of</strong><br />

chlorinated C3 hydrocarbons that is sold as a soil fumigant).<br />

Progress in improving the selectivity and efficacy <strong>of</strong> pesticides is demonstrated<br />

by the fact that application rates have decreased several orders <strong>of</strong><br />

magnitude since the beginning <strong>of</strong> the century (Fig. 3). Lower application rates<br />

also mean less exposure for those applying the pesticides in the field. Ins<strong>of</strong>ar<br />

as the increase in pesticidal activity has been matched by an increase in target<br />

species selectivity, an overall reduction in the risk to nontarget organisms<br />

(including humans) has been achieved.<br />

Although the differences in toxicity between the target species and humans is<br />

<strong>of</strong> paramount importance, other factors can influence the health hazard. As<br />

skin contamination is the most important route <strong>of</strong> exposure during pesticide<br />

application, the degree <strong>of</strong> skin penetration <strong>of</strong> a substance has a significant<br />

bearing on the risk <strong>of</strong> intoxication. The amount <strong>of</strong> active ingredient used, the<br />

6<br />

5<br />

2<br />

X sodium chlorate Herbicides<br />

S.<br />

S. --.-- Insecticides<br />

.5<br />

Fungicides<br />

lead arsenate<br />

sulphur<br />

.5<br />

.5.<br />

.5<br />

S.<br />

dinitro-o-cresol<br />

thiram " MCPAA.<br />

maneb<br />

DDT<br />

-. carbendañm<br />

Xparaquat A<br />

dimethoate<br />

'. A<br />

permethrin triadimefon<br />

DPX4189<br />

deltamethrin<br />

I<br />

148<br />

I<br />

I I I<br />

1900 1940 1980<br />

Fig. 3. Application rates (logarithmic scale) for crop protection chemicals plotted<br />

against the date <strong>of</strong> their introduction to illustrate the progressive increase in activity.<br />

Rates are representative values from the range employed in commercial practice for<br />

each compound (I.J. Graham-Bryce, Royal Society, London, UK, 1981).

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